SLC18A3, solute carrier family 18 member A3, 6572

N. diseases: 117; N. variants: 3
Disease: Myasthenias ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0947912
Disease: Myasthenias
Myasthenias 		0.110 GeneticVariation disease BEFREE Second, loss of function mutations in VAChT causes myasthenia in humans. 30003945 2018
CUI: C0947912
Disease: Myasthenias
Myasthenias 		0.110 Biomarker disease HPO